Literature DB >> 11483355

The molecular biology and nomenclature of the activating transcription factor/cAMP responsive element binding family of transcription factors: activating transcription factor proteins and homeostasis.

T Hai1, M G Hartman.   

Abstract

The mammalian ATF/CREB family of transcription factors represents a large group of basic region-leucine zipper (bZip) proteins which was originally defined in the late 1980s by their ability to bind to the consensus ATF/CRE site 'TGACGTCA'. Over the past decade, cDNA clones encoding identical or homologous proteins have been isolated by different laboratories and given different names. These proteins can be grouped into subgroups according to their amino acid similarity. In this review, we will briefly describe the classification of these proteins with a historical perspective of their nomenclature. We will then review three members of the ATF/CREB family of proteins: ATF3, ATF4 and ATF6. We will address four issues for each protein: (a) homologous proteins and alternative names, (b) dimer formation with other bZip proteins, (c) transcriptional activity, and (d) potential physiological functions. Although the name Activating Transcription Factor (ATF) implies that they are transcriptional activators, some of these proteins are transcriptional repressors. ATF3 homodimer is a transcriptional repressor and ATF4 has been reported to be either an activator or a repressor. We will review the reports on the transcriptional activities of ATF4, and propose potential explanations for the discrepancy. Although the physiological functions of these proteins are not well understood, some clues can be gained from studies with different approaches. When the data are available, we will address the following questions. (a) How is the expression (at the mRNA level or protein level) regulated? (b) How are the transcriptional activities regulated? (c) What are the interacting proteins (other than bZip partners)? (d) What are the consequences of ectopically expressing the gene (gain-of-function) or deleting the gene (loss-of-function)? Although answers to these questions are far from being complete, together they provide clues to the functions of these ATF proteins. Despite the diversity in the potential functions of these proteins, one common theme is their involvement in cellular responses to extracellular signals, indicating a role for these ATF proteins in homeostasis.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11483355     DOI: 10.1016/s0378-1119(01)00551-0

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  273 in total

Review 1.  The many dimensions of cAMP signaling.

Authors:  J H Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

Review 2.  Regulation of the transcriptional response to oxidative stress in fungi: similarities and differences.

Authors:  W Scott Moye-Rowley
Journal:  Eukaryot Cell       Date:  2003-06

3.  The stress response mediator ATF3 represses androgen signaling by binding the androgen receptor.

Authors:  Hongbo Wang; Ming Jiang; Hongmei Cui; Mengqian Chen; Ralph Buttyan; Simon W Hayward; Tsonwin Hai; Zhengxin Wang; Chunhong Yan
Journal:  Mol Cell Biol       Date:  2012-06-04       Impact factor: 4.272

Review 4.  Classification of human B-ZIP proteins based on dimerization properties.

Authors:  Charles Vinson; Max Myakishev; Asha Acharya; Alain A Mir; Jonathan R Moll; Maria Bonovich
Journal:  Mol Cell Biol       Date:  2002-09       Impact factor: 4.272

5.  Inhibition of apoptosis by ATFx: a novel role for a member of the ATF/CREB family of mammalian bZIP transcription factors.

Authors:  Stephan P Persengiev; Laxminarayana R Devireddy; Michael R Green
Journal:  Genes Dev       Date:  2002-07-15       Impact factor: 11.361

6.  Gene expression profiling of the effects of organic dust in lung epithelial and THP-1 cells reveals inductive effects on inflammatory and immune response genes.

Authors:  Vijay Boggaram; David S Loose; Koteswara R Gottipati; Kartiga Natarajan; Courtney T Mitchell
Journal:  Physiol Genomics       Date:  2016-02-16       Impact factor: 3.107

7.  Novel link of anti-apoptotic ATF3 with pro-apoptotic CTMP in the ischemic brain.

Authors:  Chien-Yu Huang; Jin-Jer Chen; Jui-Sheng Wu; Hsin-Da Tsai; Heng Lin; Yu-Ting Yan; Chung Y Hsu; Yuan-Soon Ho; Teng-Nan Lin
Journal:  Mol Neurobiol       Date:  2014-04-26       Impact factor: 5.590

8.  Reduction of spermatogenesis but not fertility in Creb3l4-deficient mice.

Authors:  Ibrahim M Adham; Thomas J Eck; Kerstin Mierau; Nicole Müller; Mahmoud A Sallam; Ilona Paprotta; Stephanie Schubert; Sigrid Hoyer-Fender; Wolfgang Engel
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

Review 9.  Regulatory SNPs and transcriptional factor binding sites in ADRBK1, AKT3, ATF3, DIO2, TBXA2R and VEGFA.

Authors:  Norman E Buroker
Journal:  Transcription       Date:  2014-10-31

10.  Inactivation of G-protein-coupled receptor 48 (Gpr48/Lgr4) impairs definitive erythropoiesis at midgestation through down-regulation of the ATF4 signaling pathway.

Authors:  Huiping Song; Jian Luo; Weijia Luo; Jinsheng Weng; Zhiqiang Wang; Baoxing Li; Dali Li; Mingyao Liu
Journal:  J Biol Chem       Date:  2008-10-27       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.